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The efficacy of delgocitinib ointment for rosacea and rosacea-like dermatitis

Single-center, open-label, single-arm clinical study to confirm the efficacy and safety of topical delgocitinib ointment in patients with rosacea and rosacea-like dermatitis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs061210078
Enrollment
30
Registered
2022-02-22
Start date
2022-06-20
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

rosacea, rosacea-like dermatitis rosasea, rosacea-like dermatitis, erythema, telangiectasia

Interventions

Continuous topical application of delgocitinib ointment twice a day for 12 weeks
delgositinib ointment, topical

Sponsors

Kajita Ai
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients aged 20 years or over at the time of agreement 2)Patient who have agreed by their own decision, with the written consent form, following the appropriate procedure of informed- consent. 3)Patient diagnosed as rosacea or rosacea-like dermatitis. 4)Patient that with refractory rosacea or rosacea-like dermatitis despite the standard treatments for 12 weeks or more 5)Patient without a history of delgocitinib ointment therapy

Exclusion criteria

Exclusion criteria: 1)Patient who have previously been treated with delgocitinib ointment. 2)Patients with any of the following disease to be differentiated: seborrheic dermatitis, atopic dermatitis (rosacea-like dermatitis arising in a patient with atopic dermatitis is not excluded), contact dermatitis, acne vulgaris, dermatomyositis, lupus erythematosus, drug eruption, lupus miliaris disseminatus faciei, eosinophilic pustular folliculitis, dermatomycosis and photo-allergy. 3)Miscellaneous: Patient who are considered ineligible for enrolling the study by a principal investigator or co-investigators.

Design outcomes

Primary

MeasureTime frame
Score of clinical manifestations eight items (hot flashes, erythema, papules pustule, telangiectasia, itch, situation, drying, edema)

Secondary

MeasureTime frame
1)presence or absence of adverse events 2) EASI score 3) NRS 4)IGA 5) Skindex-16 6)presence or absence of demodex

Contacts

Public ContactAi Kajita

Okayama University Hospital

gmd421029@s.okayama-u.ac.jp+81-86-235-7282

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026